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"61919-281-60" National Drug Code (NDC)

Famotidine 60 TABLET in 1 BOTTLE (61919-281-60)
(Direct Rx)

NDC Code61919-281-60
Package Description60 TABLET in 1 BOTTLE (61919-281-60)
Product NDC61919-281
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20140101
Marketing Category NameANDA
Application NumberANDA075805
ManufacturerDirect Rx
Substance NameFAMOTIDINE
Strength20
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/61919-281-60





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